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Recruiting NCT04515316

NCT04515316 A Room Temperature Atomic Magnetrode System for Telemetry of Epileptic Seizures

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Clinical Trial Summary
NCT ID NCT04515316
Status Recruiting
Phase
Sponsor University of Colorado, Denver
Condition Epilepsy
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2021-03-01
Primary Completion 2024-12-31

Trial Parameters

Condition Epilepsy
Sponsor University of Colorado, Denver
Study Type INTERVENTIONAL
Phase N/A
Enrollment 40
Sex ALL
Min Age 18 Years
Max Age 70 Years
Start Date 2021-03-01
Completion 2024-12-31
Interventions
OPM sensorsSQUID sensors

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Brief Summary

This study is being done to help scientists learn about the use of a device called an atomic magnetometer. The device uses sensors called optically-pumped magnetometers (OPM) which function at room temperature. This research will compare the non-invasive brain imaging application of the OPM sensors to the present SQUID-based cryogenic sensor technique used in conventional Magnetoencephalography (MEG). This study is being conducted in conjunction with the University of Colorado Boulder's Mechanical Engineering Department.

Eligibility Criteria

Inclusion Criteria: * Project A: Any adult subject, who is at least eighteen (18 - 70) years old. * Project B: Any clinical patient referred to us via the clinical MEG program, and who is at least eighteen (18 - 70) years old. Exclusion Criteria: * ONLY applicable to Project A: have a history of neurological disorders (e.g., epilepsy, Parkinson disease, Alzheimer's disease, Autism, etc…). * BOTH projects: have large amounts of metal or other magnetic field producing components present in their body or external to their body close to the measurement site, which are needed for normal functioning (e.g., metal implants, pacemakers, hearing aids, braces etc.). There is no harm to the subject with metal, it disturbs the sensor reading. Dental fillings are not excluded. * BOTH projects: pregnant women. * ONLY applicable to Project A: are not comfortable lying still for the time of the recording. * BOTH projects: are unable to offer independent informed consent to study participation.

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